Canonical Allele Identifier: CA1410887954
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150940652T= , CM000665.2:g.150940652T= GRCh38
NC_000003.11:g.150658439T= , CM000665.1:g.150658439T= GRCh37
NC_000003.10:g.152141129T= NCBI36
NG_009168.1:g.37348A= , LRG_700:g.37348A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.433+930A= MANE Select ENSP00000322280.1:n.433+930A=
ENST00000468836.2:c.581+930A= ENSP00000419892.2:n.581+930A=
ENST00000644099.1:c.426-133A= ENSP00000494762.1:n.426-133A=
ENST00000295911.6:c.205+930A= ENSP00000295911.2:n.205+930A=
ENST00000327047.5:c.433+930A= ENSP00000322280.1:n.433+930A=
ENST00000328863.8:c.434-133A= ENSP00000329158.4:n.434-133A=
ENST00000468836.1:c.205+930A= ENSP00000419892.1:n.205+930A=
ENST00000485607.1:c.97+930A= ENSP00000419244.1:n.97+930A=
ENST00000562308.5:c.104+930A=
ENST00000565169.1:c.162+930A=
ENST00000569170.5:c.162+930A=
NM_001195794.1:c.434-133A= , LRG_700t1:c.434-133A= NP_001182723.1:n.434-133A=
NM_001256819.1:c.*47+930A= NP_001243748.1:n.*47+930A=
NM_052995.2:c.205+930A= , LRG_700t2:c.205+930A= NP_443721.1:n.205+930A=
NM_174878.2:c.433+930A= NP_777367.1:n.433+930A=
NR_046380.2:n.876-133A=
XR_924167.1:n.745+930A=
NM_001256819.2:c.*47+930A= NP_001243748.1:n.*47+930A=
NM_174878.3:c.433+930A= MANE Select NP_777367.1:n.433+930A=
NR_046380.3:n.604-133A=